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crashco

01/11/18 7:32 PM

#212474 RE: DaubersUP #212472

Yeah, that’s all true but their company softball team sucks.
BP: No deal. Let our competitor buy IPIX and find a replacement power hitting right fielder. Sure they have 3 potential blockbuster drugs but they finished dead last in the New England Bio-Batters League.

Rdunn88

01/11/18 8:03 PM

#212479 RE: DaubersUP #212472

Sure, IPIX can run their own phase 3’s? Ok, if that’s the case go for it.... stop wasting time searching for partners. Tap Aspire for 50 million more and move science along. First up absssi followed by UP/OM/P and K.

keltoi

01/12/18 9:18 AM

#212536 RE: DaubersUP #212472

People seem to forget that some of the "Low hanging fruit" comes with Priority Review qualifications:Moving either one of these (K for Ped.Retinoblastoma or BOM) would generate 100's of millions in Priority Review Voucher sales to other Pharmas.

http://www.ipharminc.com/press-release/2016/11/16/cellceutix-receives-rare-pediatric-disease-designation-from-fda-for-kevetrin-for-the-treatment-of-retinoblastoma?rq=priority%

“Receiving the Rare Pediatric Disease designation strengthens our portfolio and adds to our belief that Kevetrin has the potential to provide a meaningful therapeutic benefit to children and families affected by retinoblastoma, where enucleation (removal) of the eye is often the only solution,” commented Leo Ehrlich, Chief Executive Officer at Cellceutix. “We are putting plans in place to move ahead with this exciting project. We view the voucher program as very valuable in meeting areas of unmet medical need and certainly keep in mind the monetary component considering United Therapeutics recently agreed to sell its Rare Pediatric Disease Priority Review Voucher to a subsidiary of AbbVie for $350 million.”

http://www.ipharminc.com/press-release/2016/11/16/fda-grants-fast-track-designation-to-cellceutixs-brilacidin-om-for-oral-mucositis?rq=priority%20review

The FDA established the Fast Track Designation process to facilitate the development, and expedite the review of, drugs that have the potential to treat serious and life threatening conditions and fill an unmet medical need. Drugs developed under the Fast Track program are afforded increased access to the FDA and could qualify for other programs to expedite development, including priority review and accelerated approval.

Kelt